HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24174699_24174706del , CM000668.2:g.24174699_24174706del | GRCh38 |
NC_000006.11:g.24174927_24174934del , CM000668.1:g.24174927_24174934del | GRCh37 |
NC_000006.10:g.24282906_24282913del | NCBI36 |
NG_012829.1:g.188347_188354del | |
NG_012829.2:g.213587_213594del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378454.8:c.*24_*31del MANE Select | ENSP00000367715.3:n.*24_*31del | |
ENST00000378450.6:c.*24_*31del | ENSP00000367711.3:n.*24_*31del | |
ENST00000378454.7:c.*24_*31del | ENSP00000367715.3:n.*24_*31del | |
NM_001195610.1:c.*24_*31del | NP_001182539.1:n.*24_*31del | |
NM_016356.4:c.*24_*31del | NP_057440.2:n.*24_*31del | |
NM_016356.5:c.*24_*31del MANE Select | NP_057440.2:n.*24_*31del | |
NM_001195610.2:c.*24_*31del | NP_001182539.1:n.*24_*31del |